Medical Device Manufacturer · CN , Shenzhen

Shenzhen Kentro Medical Electronics Co., Ltd. - FDA 510(k) Cleared De...

10 submissions · 10 cleared · Since 2017

Recent clearances: Transcutaneous Electronic Nerve Stimulator (KTR-2301, KTR-2302, KTR-2341, KTR-2342, KTR-2401, KTR-2402, KTR-2411, KTR-2412, KTR-2491, KTR-2492, KTR-2493, KTR-2494), Transcutaneous Electrical Nerve Stimulator For Pain Relief (Model: KTR-2302, KTR-2401, KTR-2402, KTR-2411, KTR-2412), Transcutaneous Electrical Nerve Stimulator, Model: KTR-4031, KTR-4032, KTR-4012, KTR-4015, KTR-4029, KTR-4027, KTR-4026, KTR-4021, KTR-4034, KTR-4036, KTR-4037, KTR-4039

Total

Cleared

Denied

Shenzhen Kentro Medical Electronics Co., Ltd. has 10 FDA 510(k) cleared neurology devices. Based in Shenzhen, CN.

Latest FDA clearance: Nov 2024. Active since 2017.

Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Guangzhou GLOMED Biological Technology Co., Ltd. and Feiying Drug & Medical Consulting Technical Service Group.

Shenzhen Kentro Medical Electronics Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.